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Late acute renal failure due to bilateral kidney infiltration by ALL as single manifestation of relapse after allogeneic transplantation.

机译:异体移植后复发的单一表现是ALL引起的双侧肾脏浸润引起的晚期急性肾衰竭。

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Acute renal failure (ARF) is a common complication following allogeneic hematopoietic SCT (HSCT). Numerous conditions may be associated with early ARF including pre-existing kidney dysfunction, hypertension, TBI, sepsis, sinusoidal occlusion syndrome, dehydration, acute GVHD, nephrotoxic drugs and microangiopathic syndromes, which include both thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. The incidence of microangiopathic syndromes ranges from 2 to 21% after allogeneic HSCT, and identified primary risk factors include TBI and use of calcineurin inhibitors. Clinically, thrombotic thrombocytopenic purpura tends to occur early, often within the first 90 days of transplant, whereas hemolytic uremic syndrome seems to occur much later. Direct malignant infiltration of the kidneys at diagnosis of acute leukemia is an extremely rare cause of early ARF and has been described in a few children only.
机译:异基因造血干细胞移植(HSCT)后,急性肾衰竭(ARF)是常见的并发症。早期ARF可能与多种疾病有关,包括既往的肾功能不全,高血压,TBI,败血症,正弦波阻塞综合征,脱水,急性GVHD,肾毒性药物和微血管病综合征,包括血栓性血小板减少性紫癜和溶血性尿毒症综合征。同种异体造血干细胞移植后,微血管病变综合征的发生率从2%到21%不等,确定的主要危险因素包括TBI和钙调神经磷酸酶抑制剂的使用。临床上,血栓性血小板减少性紫癜倾向于较早发生,通常在移植的前90天内,而溶血性尿毒症综合征似乎较晚发生。诊断为急性白血病时,肾脏直接恶性浸润是早期ARF的极为罕见的原因,仅在少数儿童中得到了描述。

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